Tag | Content |
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EnhancerAtlas ID | HS091-43684 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:44110190-44111660 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:44110888-44110909 | GAAATGAAAATAAAACCACAG | - | 6.12 | SOX10 | MA0442.2 | chr7:44110392-44110403 | AAAACAAAGAA | + | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_01652 | chr7:44111415-44114457 | Aorta | SE_06354 | chr7:44111271-44114877 | Brain_Hippocampus_Middle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044071 | chr7 | 44110810 | 44116089 |
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Enhancer Sequence | CACTCCAGCC TGGGCGACAG AGCGAGACTC CGTCTCAAAA AAAAAAAATT AGCTGGGCTT 60 GGTGGCTTGT GCCTGTAGTC CTAGCTACTT GGGAGGCTGA GGCAGGAGGA TTGCTTGAGC 120 ACAGGAGTTT GAGACTGCAG TGAGCTATGA TCATACTACT GCACTCCAGC CTGGGTGACA 180 GAGCAAGACC CTGTTTCTGG GGAAAACAAA GAAACAAACT ATAAAAGAAA GCAAAGAAAA 240 TCTTTGTGAT TTGGGGTCAG AGATAGGACT CCAAAAACAT AAGAAAAAAA CTGGTAAACT 300 GAATAAATTG ATAAACTGGA CTTCACAAAA ATTAAATACA TTTACTATGA AAAAAACAGT 360 GCTAAAAGAA GAAAGATAGT CTACACACTG GGAAAAAATA TTTACCAGTC ACCATAGTGG 420 CACATAAAGA ACTCTCAAGA TTGAACAGTA ACAGATGGGC ATGGTGGCTC ATGCCTGTAA 480 TCCTAGCACT TTGGGTTTTG CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCAGGT 540 GATCCACCCA CCTTGGCATC CCAAAGTGCT GGGATTACAG GTGTGAGTCA CCATGCCTGG 600 CCAACAATTC CATTTTTAAA AATGAGACTT GAACAGCCAC TTCACCAGTG AGGACATAGA 660 AGCCAGTGAA CAGATGTTCA ACGTTATCAG GCATTAGGGA AATGAAAATA AAACCACAGT 720 GAGCTACTGT TATGTACCTA CTACTAGAAA AGCTAAAGTT AACAAATACT GCAACTATCA 780 AGTGCTGACA GGGATACAGA GCAACTGCCT ACTGTGGTGT TTAACTTACA GGGGTGCTCA 840 CAACGCTGGT GGACTGCAAA ATGACAGACG CACTCGGGAC AACAACTTGG CTCTTATGAA 900 ATAAACATAT ACTTACCAAA TGACCCAGTA ATCCTGTGCC TATTTACCCA AGAGAAATGA 960 AGACCCATGT GTTACACGAA AACCTGTACA TGCATGTCTG TAGCAGTACG ATTCATCATC 1020 TCCAAACCCT GGAAACAACC CAGACTTTTT TTCTTTTTAG GCAGACTCTT GCTCTGTCGC 1080 CCAGGCTGGA GTGCAGTGGC ACAATCTCAG CTCACTGCAA CCTTGGCATC CCAGGTTCAA 1140 GCAATTCTTA TGCCTCAGCC TCCCGTGTAG CTGGGAATAC AGGTATGAGC CAACATGCCC 1200 AGCAAATTTT TGTATTTTTT GTAGAGATGG GGTTTCGCCA TGGTGGCCAG GCTGGTCTCA 1260 AACTCCTGGC CTCAAGTGAT CCACCCGTCT CAGCCTCCCA AAGTGCTAGG ATTACAGGCA 1320 TGAGCCACGG CATCCGGCCA CAACCCAGAC ATTCAACACC TGAATGGATA AACTGTAGAA 1380 CACCCATGGC ATGGAACAAA TTACAAACTC AACATACCCA GCAACCTGCA GGAACGTCAA 1440 AGGCATTAGG CTGTGGGGAG AGGCCAGTCC 1470
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